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A Novel Deletion Mutation in Proteoglycan-4 Underlies Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome in a Consanguineous Pakistani Family

✍ Scribed by Sulman Basit; Zafar Iqbal; Masha Umicevic-Mirkov; Syed Kamran Ul-Hassan Naqvi; Marieke Coenen; Muhammad Ansar; Hans van Bokhoven; Wasim Ahmad

Book ID: 113467495
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 514 KB
Volume: 42
Category: Article
ISSN: 0188-4409
DOI: 10.1016/j.arcmed.2011.04.006

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